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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Artificial Limb Components — 8 UDI-DI variants, MDR

MD Atlas
Levitate Technology ApS

Data from EUDAMED, last updated May 23, 2026

Artificial Limb Components

5715763SoleHQ

8 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Levitate Technology ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5715763SoleHQ
Device name: Artificial Limb Components
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Levitate Technology ApS
SRN: DK-MF-000046389
Country: Denmark
Email: support@letslevitate.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KFARH0WSXTAW13JWQZSM6S1H

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Shoe Essential Black/Black05715763006828
Shoe Essential White/Grey05715763006811
Shoe Essential White/Orange05715763006835
Shoe Essential White/Pink05715763006842
Shoe Gravel Black/Black05715763006774
Shoe Gravel White/Grey05715763006781
Shoe Gravel White/Orange05715763006798
Shoe Gravel White/Pink05715763006804